636-0121-00L  Single Cell Technologies

SemesterFrühjahrssemester 2020
DozierendeB. Treutlein
Periodizitätjährlich wiederkehrende Veranstaltung
LehrspracheEnglisch


KurzbeschreibungSingle-cell sequencing and imaging technologies are being applied to primary human organs and to engineered cells and tissues to understand cell states that emerge in these systems at unparalleled resolution. These technologies require sophisticated experimental and computational methods, which we will discuss in practical detail in this course.
LernzielTo understand the history and current state of the art of single-cell sequencing and imaging methods, gain experimental experience in the implementation of these methods, and to learn data analytical techniques to extract biological insight from the high-information content data.
InhaltThis course will include lecture sessions and paper discussion seminars, along with wet lab single-cell genomic experiments, followed by computational data analysis sessions based in R. In the lecture, I will cover the molecular biology and technical aspects underlying popular single-cell sequencing methods, as well as methods to spatially localize cell states within tissues or other multi-cellular systems. We will also cover the experimental aspects of light sheet microscopy and other microscopy methods as a tool to analyze cellular dynamics within complex tissues. We will read recent, seminal manuscripts in the single-cell genomics field and discuss the papers in detail as a group.

Seminar topics will include: Single-cell RNA/DNA/Epigenome sequencing, Lineage tracing, Perturbation screens, Trajectory reconstruction, Light sheet microscopy, Tissue clearing

In the lab, we will select an exciting biological phenomena to explore using single-cell sequencing and each student will get hands on experience in designing and executing the experiment, going through the steps of tissue dissociation, isolating cells, capturing and labeling nucleic acid, generating and sequencing libraries. We will then go through each step of sequencing read processing and quality control analysis, followed by sessions on data exploration (cell composition, marker gene detection, trajectory reconstruction, differential gene expression analysis, etc.)